Aqvitox Technology, s.r.o.
SK-MF-000026312 · Slovakia · Bratislava
Aqvitox Technology, s.r.o. is registered in the European database on medical devices as a manufacturer, with 12 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 12 |
|---|
Devices declared under this manufacturer
- AQVITOX-D roztok 1000 ml, fľaša
- AQVITOX-D roztok 1000 ml, vak
- AQVITOX-D roztok 1500 ml, vak
- AQVITOX-D roztok 500 ml, fľaša
- AQVITOX-D roztok 500 ml, rozprašovač
- AQVITOX-D roztok 5000 ml, bandaska
- Aqvitox - D gél 150 ml
- Aqvitox - D gél 250 ml
- Aqvitox - D gél 40 ml
- Aqvitox - D roztok 100 ml, rozprašovač
- Aqvitox - D roztok 300 ml, fľaša
- Aqvitox - D roztok 300 ml, rozprašovač
Catalogue references include 1000ml flasa, 1000ml vak, 250ml gel, 300ml rozprasovac, 40ml gel, 5000ml bandaska.
European nomenclature codes declared: M04041503.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 12 |
| Country of registration | Slovakia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 12 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. Aqvitox Technology, s.r.o. was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
2024-MDR/QS-012/A | supplemented | 2029-03-20 |